A Standardised Procedure for Surveillance and Monitoring European Habitats R.G.H. Bunce1, J. Brandt2, G. de Blust3, R. Elena-Rossello4, G.B. Groom5, L. Halad6, G. Hofer7, D.C. Howard8, R.H.G. Jongman1, P. Kovar9, M.J. Metzger10, C.A. Mucher1, E. Padoa-Schioppa11, D. Paelinckx3, A. Palo12, M. Perez-Soba1, I. Ramos13, P. Roche14, H. Skanes15 and T. Wrbka16 1Alterra Green World Research, Wageningen, The Netherlands; ; 2Roskilde University, Department of Environmental, Social and Spatial Changes, Roskilde, Denmark; 3Institute of Nature Conservation and Forestry Management, Brussels, Belgium; 3Polytecnic University of Madrid, Department of Forestry, Madrid, Spain; 5NERI, Department of Wildlife Ecology and Biodiveristy, Roende, Denmark; 6Institue of Landscape Ecology, Slovak Academy of Sciences, Bratislava, Slovakia; 7FAL, Zurich, Switzerland; 8CEH Lancaster, UK; 9Charles University, Faculty of Science, Prague, Czech Republic; 10Wageningen University, Department of Environmental Systems Analysis, Wageningfen, The Netherlands; 11University of Milan, Department of Environmental Science, Milan, Italy; 12University of Tartu, Tartu, Estonia; 13CESUR, Lisbon, Portugal; 14University of Aix en Provence, Marseille, France; 15Stockholm University, Department of Physical Geography, Stockholm, Sweden; 16University of Vienna, Institute of Conservation Biology, Vegetation Ecology and Landscape Ecology, Vienna, Austria; Corresponding author: bob.bunce@wur.nl Contents Abstract ...................................................................................................................................... 3 Introduction ................................................................................................................................ 4 The Conceptual Principles ......................................................................................................... 6 The Surveillance System ........................................................................................................... 8 Validation ................................................................................................................................. 14 Discussion ............................................................................................................................... 18 References .............................................................................................................................. 20 Abstract There are well defined scientific and policy requirements for a practical, transmissible, and reproducible procedure for surveillance and monitoring of European habitats. A procedure is described that will satisfy these requirements and which can provide the necessary data that are currently lacking. Rigorous rules are required; otherwise changes from baseline records cannot reliably be separated from background noise. The procedure is based on classical plant Life Forms, used in biogeography since the nineteenth century, and on the underlying statistical correlation between these Life Forms and the environment. This relationship has been validated statistically and the procedure has also been tested in the field in all European environmental zones. 130 General Habitat categories are described and these are enhanced in the field by recording environmental, site and management qualities to enable flexible database interrogation. The same categories are applied using rules, with appropriate qualifiers, to areal, linear and point features, so that for the first time integrated reporting of variation of habitats at the landscape level can be carried out. It therefore incorporates landscape ecological principles such as landscape diversity and will enable both connectivity and fragmentation to be assessed at the detailed landscape level. Keywords: field recording, surveillance, habitat, monitoring, stratification, biodiversity, Life Forms Introduction The current primary policy requirement in NATURA 2000 sites is to assess the favourable conservation status and extent of selected species and habitats. This requires a reliable, comparable and repeatable method for monitoring changes in species and habitats, both within and outside, NATURA 2000 sites. However, monitoring is also needed for other initatives, such as indicators of sustainable development and biodiversity action plans. Currently not only are consistent data not available to answer these requirements, but also a standardised rule based procedure is not available. The approach described in the present paper fills this gap and is based on the BioHab project carried out in the EU Fifth Framework programme (EVK2-CT-2002-20018). Whilst the core of the procedure concerns rules and instructions for consistent field recording, it is essential that they are linked to a spatial framework for the whole of Europe. [Ramon’s diagram here of pstial and temporal issues]. Such a framework is therefore integral to the methodology as it provides a means to extend the detailed samples needed to assess habitats in the field to European estimates. A summary of the framework is also therefore provided. The temporal dimension is added by describing the monitoring procedure. Field recording has been at the core of ecology since its inception as a recognisable science. Long-term monitoring is more common in species oriented approaches e.g. birds and carabid beetles (Den Boer and Van Dijk 1994). The development of vegetation science as part of ecology has been mainly descriptive and based on the selection of homogenous stands of vegetation, usually relatively undisturbed (Braun-Blanquet 1932; Tuxen 1937). Such work is not designed for long-term monitoring, although the individual records are suitable, if they are relocateable (e.g. Grabherr et al. 1994). Long-term vegetation monitoring studies are restricted. For example, in the UK (Bunce et al. 1993) found under five case studies of longterm vegetation monitoring. Similarly, quantitative ecologists, e.g. Greig-Smith (1964) were largely concerned with technical, as opposed to actual practical problems. Bunce and Shaw (1973) described a standardised procedure, which was applied to British woodlands in 1971 and subsequently repeated in 2003 (Kirby et al. 2005) demonstrating that statistical rigour is essential for long-term monitoring. However, all these approaches do not involve recording at the landscape level i.e. involving complexes of habitats, as described by Sheail and Bunce (2003) and Fjellstad et al. (2001). Any procedure must recognise and utilise this complexity – hence the development of the present approach. In contrast, most European approaches to the assessment of habitats either ignore these requirements, or deliberately avoid landscape complexitiy by selection of sites that are considered homogenous. In the 1950’s and 60’s, the development of the ecosystem concept was restricted, albeit not explicitly, to concepts of vegetation classification. However, in the 1980’s it gradually became recognised that, whilst habitats had strong links to vegetation classes, they could also be independent. This was partly because animal ecologists found that vegetation structure often overrode vegetation classes but also partly because some widely recognised habitats were not directly linked to traditional vegetation associations. This situation has recently been recognised by Rodwell et al. (2003) showing that the match between the European Habitat Classification (EUNIS) (Davis and Moss 2002) and vegetation assemblages is often indistinct. In the 1980’s therefore, habitat mapping progressively became a separate exercise from recording vegetation alone because strategic conservation priorities did not necessarily involve the distinction between vegetation associations. For example, the small biotope project in Denmark (Agger and Brandt (1988) monitored changes in small landscape patches in intensively farmed landscapes, with minimal relationships with vegetation associations. Similarly, the Phase 1 Habitat Survey in England (JNCC (1990)) enabled rapid mapping to be carried out over large areas to provide a strategic basis for determining conservation priorities albeit at a low level of detail and consistency. Similarly, an examination of the development of the Countryside Survey in the UK (Haines-Young et al. (2000)) shows that although it initially concentrated on vegetation in 1978, by 2000 the reporting of status and change was based on 19 Broad Habitats. Whilst this project has shown the essential role of vegetation records in determining quality (i.e. favourable conservation status) it has also demonstrated that habitats are convenient for reporting. Furthermore, the habitat names are more often than vegetation classes understandable by policy makers. . Landscapes usually contain complexes of habitats whereas at the habitat level below contain mixtures of vegetation associations. The list of CORINE Biotopes (Devillers et al. 1991) was derived from expert group discussions. It was largely based on vegetation classes and mainly concerned semi-natural habitats. Both Annex 1 of the European Habitats and Species Directive and the subsequent Palaearctic classification (De Villers and Devillers-Terschuren (1996) have strong links to the CORINE Biotope Classes. More recently, EUNIS (Davies and Moss (2002) whilst still maintaining strong links to the previous classifications, also introduced classes for artificial and highly disturbed situations. The present project originally intended to develop rules for the EUNIS classes but concluded that many terms used in the key e.g. montane and subMediterranean were not sufficiently well defined for determining the classes in the field and for subsequent monitoring. Accordingly, the approach developed adopted traditional scientific principles in developing General Habitat Categories based on plant Life Forms, appropriate for monitoring and reporting consistently as the European scale. The present paper first describes these principles and the validation process accompanying them. The surveillance system is then described with a summary of the principal rules and the method of recording qualifiers to convey information on drivers and descriptive characters. Finally, the environmental framework for relating the necessary detailed samples to the whole population is described. Additional details on structure are also provided to provide better links of in situ to remote sensed information. The Conceptual Principles Originally plant Life Forms were identified as valuable in the project because they provided rules to separate grassland, scrub and forest categories using rules that could be applied consistently in the field. However, during the project it became clear that Life Forms provided a means of transcending species and enabling consistent recording of habitats to be undertaken. It is generally recognised that at the continental level biomes need to be defined in terms of the physiognomy of the dominant species and that Life Forms are necessary because individual species are too limited to encompass widely dispersed geographical locations (Woodward & Rochefort 1991). It was also realised in the project that the adoption of Life Forms would provide links between European categories and other studies of global change that use biomes based largely on Life Forms e.g. Mediterranean scrub in the western USA, Chile, South Africa and Australia. By contrast, many criteria have been used to construct existing European habitat classifications e.g. species, geographical distribution, vegetation classes and environmental factors. It was therefore decided to use Life Forms as the sole criterion for determining the primary General Habitat Categories (GHC’s) so that they can be recorded directly in the field but can also be sufficiently robust to be used to link existing datasets which have been collected for monitoring. The basis of the GHC’s is the classification of plant Life Forms produced by Raunkiaer (1907; 1934). The underlying scientific hypothesis is that habitat structure is related to the environment on a European Scale, or even locally if there is a sufficiently wide range of conditions. The application of the Environmental Stratification (Metzger et ai. 2005; Jongman et al. 2006) provides a sampling framework linked to climate, topography and geographical location, which can also be tested statistically. Various floras were consulted, especially Clapham et al. (1952) and Pignatti (1982) to determine at what level to treat Life Forms as some recent floras e.g. Oberdofter et al. (1990) give highly detailed categories. However, as Raunkiaer (1934) originally emphasized, the more detailed breakdown of Life Forms, loses the strong relationship with climate. Eventually, it was decided to use 16 Life Forms (Herbaceous and Tree/scrub, see Table 1) with the plant height ranges taken from more recent literature Ie.g. Castri et al. (1981); Quetzal & Barber (1982). The main problem was however, with Gramineae, Cyperaceae and Juncaceae, where many species have rhizomes, which are primarily for vegetational reproduction not for perennation. There are also differences between the attribution floras of Life Forms as well as difficulties in the determination of the actual position of the rhizomes or stolons in the field. It was therefore decided to group these three taxa together as “caespitose hermicryptophytes”. Further details and examples of the species in the 16 Life Forms are given in Bunce et al. (2005). It is also recognised that some species are sufficiently plastic to adapt to several habitats, e.g. Ranunculus aquatilis; in which case the environmental conditions present at the site, as described below should be used to determine whether, for example, it is in aquatic or waterlogged conditions. Another aspect of plasticity relates to woody species as shown in Table 2 which respond to a range of environmental and management pressures. These species can occur in lower than optimum height categories because: They have been heavily grazed They have been burnt They are regenerating They are in highly exposed or extreme environments The first three categories are transitional and shifts can take place according to changes in external pressures e.g. fire or felling. The fourth is a climax state. The only way to provide consistent data is to record the actual hights of the tree and shrub cover in the field, because otherwise the potential height is a matter of judgement. There is a functional relationship between the Life Forms and pathways of change over time e.g. from tall shrubs 2-5m to forest trees over 5m which are then quantifiable, as in the flow diagrams beween habitats given by Haines-Young et al. (2000). Land associated with built structures and routes of communication (termed urban in a broad sense) and crops cannot be defined solely in terms of Life Forms as they are primarily land uses. However, for policy and practial reasons it is essential that such land is separated from other land covers that are mainly in agricultural or forest use. Hence, these two categories have been separated at the first level of the hierarchy (Bunce et al. 2005), together with bare land as shown in Table 1. However, within both the former categories, subsequent divisions are then based on life forms at the second level of Table 1. These are termed super categories. A major problem in habitat classifications is how to determine the number of classes. In some habitat classifications by e.g. Fernandez (2003) there are almost 1000 classes and in EUNIS there are 350 at level three. It was therefore decided that below the first tier of five super categories all possible combinations of Life Forms should be included, even although some will be rare (Table 1). This procedure has provided a statistical rule for determining the number of General Habitats Categories (HGC’s) and results in 130 covering the pan-Euroepan region, except Turkey. Other Life Forms e.g. tall succulents would have to be included for a larger region but at present they are included as qualifiers. Other qualifications to be GHC’s are discussed below. The principal reason behind the GHC’s is that they enable the primary decision on the habitat categories to be made in the field and the rules and instructions also make them appropriate for monitoring. A worked example of monitoring national change using a similar level of categories of habitats is given by HainesYoung et al. (2000). The Surveillance System General Habitat Categories The General Habitat Categories are designed for recording habitats and providing links to their classifications. The General Habitat Categories are based mainly on Life Forms with added detailed information on environment, site, management and species composition. They are designed for consistent recording as described by Bunce & Shaw (1973) and are based on the same principle of using explicit rules. The success of these rules in long-term monitoring has been shown by Kirby et al. (2005). Because GHC’s are fundamental ecological categories, the transfer between them can be readily defined as shown in Figure 3 and as explained above. The working definition of “habitat” developed by the BioHab project (Bunce et al. 2005) is as follows: “An element of land that can be consistently defined spatially in the field in order to define the principal environments in which organisms live”. General Habitat Categories (GHC’s) have been developed in order to enable consistent recording of habitats by defining basic mapping units that can then be re-surveyed after a given time interval (Table 3). It is preferable to carry out preparatory work on delineation of the major elements within the survey area from the aerial photographs and related material, e.g. cadastral maps, to assist the mapping process, otherwise it has been shown that differences in base maps between countries do not enable consistent mapping. Details of the practical mapping procedure are given in Bunce et al. (2005). The recording procedures are determined in advance to ensure standarised data as shown in Table 4. All major decisions should be made in the field rather than being postponed to the laboratory to improve consistency. Data mining through database management methods can however be used to extract other data, e.g. calculation of slope angles, aspect and height of cliffs, land units of ownership. For survey, the recording of the GHC’s should be made in a time window either side of the period of maximum biomass, i.e. as close as possible to the height of the growing season. The monitoring should be carried out as close as possible at the same date (Barr et al. 1993) as it has been shown that date is the main source of error. This window is likely to be fore maximum biomass in the Mediterranean, but after in Scandinavia. The extent of the window needs to be set by region, using local phonological information and differs between Environmental Zones, Environmental Strata and countries. Some local flexibility may be required for annual variations in seasons and weather. Environmental terms must be considered at a contintental scale e.g. “dry” in Scotland may be “mesic” compared with southern Italy. This means that no continent wide survey can be carried out without adequate field training for all surveyors to ensure that terms are fully understood. Combined teams of two people, probably with a botanist and an experienced mapper, are needed to ensure that optimal expertise is available. Quality assurance and control are essential and should be carried out regularly with standard protocols, as described by Barr et al. (1993) and Kirby et al. (2005). In the BioHab project, it was decided to apply the same recording format to be used for areal, linear and point elements. This procedure not only uses fewer categories to be used but also enables reporting to be more readily understood. It also helps express the contrasts between different types of landscapes where areal and linear features make contrasting contributions to diversity. Project qualifiers are recorded in seven sequential fields, as described in Table 5. These can consist of data recorded in the field as well as through database management. In total the recording form has an alpha identifier and eight subsequent recording fields (Table 5). The determination of the GHC is based upon a sequence of four dichotomous divisions related to a set of five super categories as shown above, which determine the set of Life Forms that can be used to identify the appropriate GHC. The first decision concerns whether the element is Urban, the second whether it is a Crop, the third whether it is Sparsely Vegetated and the fourth whether it is Trees or Shrubs (Table 6). Rules have then been added for further divisions in all super categories and habitat categories including percentage criteria. New areal or linear elements are separated from adjacent or surrounding areal elements based on pre-defined rules as described by Bunce et al. (2005). Environmental Qualifiers Environmental and global qualifier codes are essential information for detailing GHC’s; they are therefore entered into the second field of the habitat recording sheets for areal and for linear elements and they express variation between elements that have the same GHC. They are not applied to urban/constructed, crop or sparsely vegetated elements. The moisture categories are based on Pyatt (1999) and are defined in a European gradient as shown in Table 7. The second environmental gradient is determined on nutrient levels in the soil. These were originally developed for Central Europe by Ellenberg (1992) using expert knowledge of the environmental amplitude of individual species. The species have been recalibrated for Britain (Hill et al. ####) and are available on the web (htt://science.ceh.ac.uk/products_services/software/mavis.htm). However, Ellenberg values are not available for some regions, so local experience of the ecological amplitude of species may be needed, especially in the Mediterranean. Ellenberg values are available for fertility, acid/basic gradient and salinity. Fertility is often localised along landscape elements e.g. rivers and around feeding troughs. For ease of recording a matrix as shown in Table 8 is used to determine codes. Indicator species can be used to identify such elements e.g. Urtica spp., Stellaria media, Galium aparine, Stachys suylvatica and Rumex alpinum. The two highest levels of Ellenberg fertility values are combined because lower levels are too difficult to record in the field without a full species list. Indicator species can also be used for the acic/basic gradient values and can be supported by knowledge of the soil/rock type, landscape context and if necessary, by testing the soil reaction. Salinity can be assessed by the presence of halophytes e.g. Salicornia spp., Puccinellia spp and Spartina spp. Care is needed with some species e.g. Armeria maritime and Plantago maritime as they also grow in mountains away from saline conditions. Brackish conditions can be determined from the landscape context and the presence of some species that are some degree tolerant of salt e.g. Agrophyron repens and Zannichelia palustris. Whilst there is an element of judgement in assessing the position of a given element on these gradients, they are mainly stable and when monitoring changes should only be recorded if there is supporting evidence e.g. flooding for a different position in the matrix. For all cells in the matrix the overall balance of species should be used, not individual indicators. Other codes are also provided, as described by Bunce et al (2005). Environmental qualifiers are determined for each mapped element except for the urban, sparsely vegetation and crop super categories. Site qualifiers are recorded in field three including factors such as geomorphologic features and coastal attribute. Management qualifiers are grouped in convenient sections e.g. forestry and reacreation and are designed to given information as potential causes of change. The detailed information of the areal and linear elements, the main plant and crop species associated with each recorded alpha code are recorded. Life Forms with a cover of at least 10% are also recorded. The species that constitute at least 30% cover of the vegetation (as seen in vertical perspective) of each Life Form that has been recorded in the first column of field five are recorded, as well as the percentage cover. Three further fields are provided for pan-European habitat classifications e.g. EUNIS, local habitat classifications e.g. MorilloFernandez (2003) and for phytosociological associations. All the above data can be recorded on a hand-held computer and a pilot system was developed in the BioHab project. Mapping Units and Areal Elements One of the main problems in determining the number of samples is that a given habitat often occurs at different scales in contrasting landscapes. The recording procedure therefore needs to reflect such heterogeneity. In the present paper, it is recognised that the optimum size of the sampling unit depends on the objective of study (Lambert 1972). The choice of scale is therefore a compromise between sampling many small units, as opposed to fewer larger units. As discussed by Bunce et al. (1996) it costs more to sample many small units although they may give more precise estimates (Gallego 2002). More systematic inclusion of variations due to management might have been an argument for larger units (Brandt et al. 2002), but the 1 km square is a convenient compromise sampling unit for many purposes as there is no optimal size for all the habitats and landscapes at a continental scale because of the variation at both landscape, patch scales and management scales, then it is optimal to use a standard size, which then enables the direct comparisons to be made of relative heterogeneity. The 1 km square unit also enables internal spatial modelling of habitat patches and is sutiable for scenario testing (Bunce et al. 1993). In terms of the General Habitat Categories where a given category is in an optimum situation for its development, it will occur extensively e.g. dwarf shrubby Life Forms below 0.05 m in the Scandinavian mountains (Alpine North). In the Alps (Alpine South) it may occur as small patches but not at all in most of Europe. Table 2 shows an example of how a given habitat may occur in different landscapes. This complexity means that for any given survey, the strategy has to be at a constant scale to enable comparison of relative extent to be made. Subsequently, as described by Barr et al. (1993) further samples can be increased to reduce standard errors, once the initial validation has been assessed. Alternatively, rare habitats, of which the distribution is often known, can be targeted, either objectively using known parameters e.g. coastline, or within patches identified in the field. In the latter case, statistical estimates of extent cannot be made, but at least rare habitats can be monitored in this way. Tests in BioHab of recording point information at intersections, as in the LUCAS project programme (Gallego 2002) showed that not only spatial information was not produced but the essential link to satellite imagery could not be made. The Minimum Mappable Element (MME) is 400 m2 (with minimum dimensions of 5 x 80 m), based on experience in the GB Countryside Survey (Barr et al. 1998) and in field trails in 1998 and 1999 in El Tiemblo near Madrid, Spain. This contrasts with the 250 000 m2 of the CORINE land cover map and 2500 m2 of the Biopresss Project (http://www.creaf.uab.es/biopress/index2.htm). However, such detail is essential to express the landscape ecological characteristics of many landscapes especially in the Mediterranean region. Within Bunce et al .(2005) detailed rules are provided for mapping e.g. for elements which cross the boundaries of the 1 km2 and the use of interpreted aerial photographs to provide initial boundaries for mapping. Some elements e.g. canals, motorways or major rivers may be mapped as areal elements according to the rules, but may be subsequently allocated to linear features by database management for specific objectives e.g. Haines-Young et al. (2000). The fundamental principal is that disaggregated data are collected, so that subsequent analysis can produce statistics that are sufficiently flexible to answer a range of policy requirements. Linear and Point Elements In the majority of literature referred to above both linear and point features are largely omitted. This also applies to most phytosociological studies e.g. in the Czech Republic over 30,000 relevees have been recorded, none of which are on linear or point features. However, many studies have shown that especially in intensively managed agricultural landscapes biodiversity has progressively become restricted to such situations e.g. Bunce & Hallam (1993) and Hermy & de Blust (1997). Moreover, as intensification continues, so does the pressure increase even in such limited areas e.g. Haines-Young et al. (2000) and Agger & Brandt (1988). Furthermore, many cultural landscapes are exceptionally rich in linear features largely the product of management by managing the terraced landscapes of Crete and the dense hedgerow network of the bocage. It is therefore essential not only to assess the resources of linear and point elements in representative landscapes but also to monitor change. As with areal elements a series of rules and protocols have therefore been developed to maintain consistency and repatability as described by Bunce et al. (2005). A linear element states that it must have a width of metre less than 5.0 m but more than 0.3 m and must be longer than 30 m which is the Minimum Mappable Length (MML). Elements that are smaller than 400m2 and shorter than 30 m can be recorded as points. Linear habitats often occur as complexes e.g. a fence, a ditch and a hedge, in which case instructions are provided for mapping. It is recognised that in many cultural landscapes the number of point features can be very large e.g. trees along hedgerows and patches of rocks in fields. Two guidelines are provided for recording such points: 1. Point features which add to landscape diversity, usually because they represent a particular habitat which is generally absent from the surrounding area e.g. rock outcrops or boulders in a grass field. 2. Point features which affect the ecological function of landscapes e.g. drinking places in grasslands or weirs in watercourses which hinder migration. However, a given survey may decide to omit point features and the procedure followed should be recorded. Validation Previous experience in field workshops organised by the International Association for Landscape Ecolgy (IALE) showed the difficulties in mapping theoretical classifications e.g. EUNIS and CORINE Biotopes in the field, especially where continuous gradients were concerned. It is therefore essential that rules were tested rigorously in the field in a variety of situations. Not only are many terms not defined but also sufficient detail is not provided for consistent definition. In the case of Priority and Annex 1 Habitats especially, it was shown that further information would be required e.g. on the natural distribution of critical species before they could be recorded. Excursions were made to diverse biogeographical locations e.g. in Almeria in south-east Spain and inside the Arctic Circle in northern Norway, as shown in Figure 1. These excursions were selected to ensure that all major combinations of Life Forms were present within the represented GHC’s. The rules were then discussed in the field and mapped in 1 km squares in a range of workshops varying from Tessaloniki (Greece), Faro (southern Portugal), El Tiemblo (central Spain), Poprad (Slovakia) and Uppsala (eastern Sweden). These practical excursions and the exposure of the mapping procedures to external comments led to progressive refinement of the field instructions and has ensured that the rules are sufficiently robust to be applied across Europe. Some categories are rare and may never cover areas over 400 m2; hence the importance of recording linear features and points to express the variation at the landscape level. As the use of Life Forms is based on a regression model, the hypothesis can be tested, although it is the substance of classical biogeography e.g. Walter (1973) and Woodward (1991). The first such test was carried out in a valley in the Picos de Europea, north-west Spain, which extended from broadleaved evergreen forest at 200 m to scree, rock and subalpine vegetation at 2500 m. Orthogonal regression, as described in the context of land classification by Bunce et al. (1996), was used to calculate the correlation between mixture of Life Forms in stratified random samples drawn from eight environmental strata using the mean altitude of each strata as the independent variable. The correlation coefficient was 0.94 (6 df) and highly significant showing that at even a local scale the model was valid. In the second test the data for elements used was that which had been collected on the proportion of Life Forms from patches of > 400 m2 visited during the field excursions and workshops. These data can only act as a demonstrator as they are not collected from representative random samples. The results are shown in Figure 2 and support the principle of Life Forms and their relationship with the environment as expressed by Raunkiaer. The results also show that in practice there are several significant dimensions e.g. from bare rock to annual vegetation (high mountain to Mediterranean) and from grasses to spiny cusions (temperate to Mediterranean). The axes are linked to the main environmental sectors of Europe, as described by Metzger et al. (2005) and Jongman et al. (2005) showing that Alpine North (Scandinavian mountains) and Mediterranean South (extreme southern Europe) were isolated and the other zones clustered together showing the influence of management. This analysis shows that Life Form combinations are more important than the individual categories. They form complex relationships with the environment on the one hand but also show modified patterns because of management by man on the other. Stratification The early part of this paper shows the level of decision making needed to make consistent records as shown in Figure 1. Spatial and temporal aspects need to be concidered. The present section deals with stratification to provide the former and the next section with the latter. The collection of the field data must be based on a statistically sound sampling design so that it is independent and unbiased, as outlined by Bunce et al 1996. A stratification of framework has been constructed that optimises the selection of sampling locations. Previous experiences (Bunce et al 1996) has used independent environmental classifications derived from existing biogeoclimatic information. This approach has been developed in Great Britain (Sheail and Bunce 2004) but also in Spain (Elena Rossello1997). It is likely to be also efficient at a continental scale eg in Australia (Cawsey et al 2002). The stratification (Metzger et al 2005, Jongman et al 2006) has been derived from a statistical analysis of climatic and topografic data at a 1 Km square resolution. 13 environmental zones have been established linked hierachically to 84 environmental Strata. This classification can be used to select the minimum of about 1400 1 km squares that would be required to obtain statistically reliable estimates of the extent of GHC’s for Europe. Existing data from objectively located samples can also be integrated where possible. This method enables data from sample squares to be integrated first at the Stratum level and then eventually for the whole of Europe by adding the figures from the Strata. Standard statistical procedures, as defined by Barr et al 1993, can be used to obtain standard errors for individual Strata for Europe. The data from the samples could also be linked to satellite imagery based information e.g. the CORINE land cover map to improve the interpretation of the categories. Monitoring Monitoring involves the temporal dimension referred to in Figure 1 and involves repeated measurements at different time intervals. It is statistically essential to return to the same sites to record changes (Barr et al. 1993, Brandt et al. 2003). This is the procedure followed in all the major monitoring exercises in Europe. There are several networks already existing for monitoring environmental changes employing various size units from 16 km squares down to 0.25 km squares, and sample extents that generally comprise between 0.2 and 0.3 % of the spatial extent of the associated populations (Brandt et al. 2002b). Most of the field recording is at the 1 km square level, as a compromise between detail and generality, and the BioHab has therefore been based at this level. The General Habitat Categories are specifically designed to be recorded consistently in order to produce statistically robust estimates of extent. However, consistency becomes even more imperative when the recording and mapping of change is concerned. The majority of field habitat mapping exercises involve surveillance and are not designed to record change. More stringent criteria are required in order to ensure that real change is recorded and not results that are distorted by differences between observers and of recording technique. This requires that emphasis in the re-survey be placed on registration of changes compared with the recordings made previously e.g. the procedure used in Brandt & Agger (1988). Thus, information from the previous survey forms the basis for the field mapping and recording in the re-survey, which is implemented as a check for change of each element recorded in the previous survey. Change detection by independent surveys and subsequent data analysis is time-consuming and can lead to uncertainties about whether the changes detected are real or statistical artefacts. Such monitoring has many advantages, especially when seen in the long-term, as it allows checking of the quality of each of the surveys. Each registration of a change generates the question: is it a real change? Or is re-evaluation of the earlier registration required? This permits a higher degree of confidence in the data as the number of surveillance events increases. The result of this procedure is that the monitoring has not only become more reliable, due to better registration techniques, but also the editing of former registrations has added to the quality. In fact, a considerable part of the time needed for the refinement of the database in a Danish national landscape monitoring system made every 5 years from 1981 to 2001 has been devoted to the systematic control of all detected changes back in time (Brandt et al. 2002a). Such a rigorous control is necessary, since landscape monitoring relies on the detection of small changes and using this procedure guarantees that the changes have actually taken place. The statistical confidence that can be attached to the measures can however be low if changes are rare. There is much experience in applying such methodology in the detection of change e.g. Northern Ireland, Denmark and Great Britain, and in interpreting changes from aerial photographs e.g. Spain, Sweden and The Netherlands. One of the key elements of this approach is the detection and evaluation of alternations within habitat types, e.g. new forestry planted on blanket bogs is negative, but is positive if taking place on arable land (Figure 3). Data Quality and Quality Control Whilst it is recognised that the information on management is more difficult to record than the GHC’s, Kirby et al. (2005) have shown that such data can reveal significant changes if the sample is sufficiently large. Also it is not necessary to always have data collected in the same sites, as Bunce et al. (1999) showed for moths and freshwater invertebrates. In addition data from socio-economic surveys could be linked via the Environmental Strata of Metzger et al. (2005) by providing the boundaries of the strata to third parties who hold confidential information. The various sets of qualifiers described above are considered provisional, and additional categories could be added by consultation with regional experts. It is also recognised that the descriptions would need to be improved to make them fully understood across Europe. Further details could also be added on landscape character and geomorphological features. Barr et al. (1993) and Kirby et al. (2005) both showed the importance of time of year that the records are made. Detailed contingency plans are therefore needed to ensure that the data of survey in individual regions are not only time for phenology but also for variations between years. This is most likely to be important in the Mediterranean region where variation is generally greater between years than elsewhere. Quality control and assurance are essential to ensure reliable data. Quality control procedures involve checking field surveyors identification and mapping skills by experienced staff actually in the field. Whilst this is most important during the early stages of the project, it is also essential throughout and should include independent random checks of individual samples. This was carried out in the UK Countryside Surveys in 1993 and the results compared using primary codes of major habitats, comparable to GHC’s and land use (Barr et al. 1993). Analysing these codes showed a correspondence of 84% (95% in fields; 71% in open vegetation). The only directional bias was the distinction between heaths and bogs, which are now included only as qualifiers. The differences were mainly due to the actual data of the survey, which has led to future surveys being carried out at the same date as the baseline. The secondary codes (comparable to qualifiers in the present paper) had 75% correspondence. The conclusion was that the data were sufficiently robust to detect change and implicitly, that the approach described in the present paper will also be able to detect change. Discussion The Policy Background Since the Rio Convention on Biological Diversity was signed by 150 governments after its agreement in 1992, there have been a series of policy initiatives relating to biodiversity. One of the issues in conserving in situ biodiversity is the conservation of threatened habitats as laid down in the European Habitats and Species Directive (Council Directive 92/34/EEC). A full review of all initiatives and actions is beyond the scope of the present paper, which primarily concerns habitats within the biodiversity hierarchy but could be extended to vegetation, species and genetic levels of biodiversity. Within the Directive, the conservation of habitats is elaborated in article 2, 3 and 4, with an extensive list of habitats of European importance and priority habitats for conservation given in Annex 1. This list of habitats was derived form the CORINE Biotope project which was initiated in 1986 but reported in 1991 (Devillers et al. 1991) and led to the list of habitats in the Directive, within which certain Priority Habitats were identified for legal protection. This list has been progressively modified by expert consultation following addition of new accession states e.g. Finland and Austria. The Directive has been subsequently augmented by other initiatives e.g. the Gothenbug Commitment by the EU, that biodiversity decline should be halted by 2010. All of these iniatives are needed in support of a baseline database, using extant information and both for assessing the extent of habitats and as well as new data and subsequent monitoring. Such a baseline is currently lacking and projects such as MIRABEL (Petit et al 2001) have only been able to use expert judgement for assessing the distribution and extend of European habitats. Mucher et al 2004 have used the descriptions in Annex 1 to derive rules using existing databases to predict distribution of habitats. However, many of the descriptions do not contain enough detail for mapping. Over recent years the Natura 2000 series of sites has been set up as the major initative to maintain habitats and their associated biodiversity. The selection of these sites is primarily based on Annex 1 Habitats but also reflects national priorities. However, inevitably such sites can only cover a small proportion of the European land surface (probably about 10%); outside their boundaries there is limited or no protection of habitats. Nevertheless, the non- designated land not only contains a high proportion of the total wildlife resource, but is actually what most people experience in everyday life. It is therefore essential for a panEuropean procedure to adequately define rules to record habitats on such land, as well as the mainly semi-natural habitats of Natura 2000 sites, hence the development of the present procedure. It is also essential to provide an objective baseline as described in the present paper against which the effectiveness of protection within Natura 2000 sites can be measured. None of the existing procedures adequately covers the complexity of landscapes nor the recognition of the spatial heterogeneity across Europe. Although the Natura 2000 network is based on Annex 1 and Priority Habitats, some countries e.g. Spain have interpreted the remit in a broad way. In addition the interpretation of the habitat types also varies between countries. This is partly because the types themselves are derived from a mixture of general information and phytosociological classes and also because they are in response to different national priorities. In general, the individual species provided in the Annex 1 descriptions should not be used alone to identify habitats, but rather a complex of associated species, although again this is difficult to apply consistently. The current database in Natura 2000 is difficult to use, because inconsistencies may be due to national interpretations or even data errors. There are also gaps in the series e.g. Calthion in The Netherlands, which have been added to the nearest class but this has not been carried out consistently across the EU. Many of the types are of such restricted distribution that they cannot be picked up by random or grid samples. Instead a series of individual stratifications and masks eg. Coastal would be required. An initial trial has shown how the GHC’s could provide the necessary framework by reducing the uncertainty in the identification of Annex 1 habitats, for which at present there is no key and inadequate descriptions eg 9260 Castanea sativa woods have three lines whereas 6230 species rich Nardus grasslands have three pages . A possible approach is to develop an expert system which can then be circulated to regional experts to add their local knowledge. References Agger, P. & Brandt, J. 1988. Dynamics of small biotopes in Danish agricultural landscapes. Landscape Ecology 1: 227-240. Barr, C.J., Bunce, R.G.H., Clarke, R.T., Fuller, R.M., Furse, M.T., Gillespie, M.K., Groom, G.B., Hallam, C.J., Hornung, M., Howard, D.C. & Ness, M.J. 1993. Countryside Survey 1990: main report volume 2. Department of the Environment, London, 174pp. Barr, C.J. 1998. Countryside Survey 2000 Field Handbook. Centre for Ecology and Hydrology, Grange-over-Sands, U.K. Braun-Blanquet, J. 1928. Pflanzensoziologie: Grundzuge de Vegetationskunde. Springer Verlag, Berlin, 330pp. Bunce, R.G.H. & Shaw, M.W. 1973. A standardised procedure for ecological survey. Journal of Environmental Managmeent1: 239-258. Bunce, R.G.H. & Hallam. C.J. 1991. Diversity of vegetation in British landscapes. In: Pineda, F.D., Casado, M.A., de Miguel, J.M. & Montalvo, J. (eds), Biological Diversity. Fundacion Ramon Aceres, Madrid, pp 77-81. Brandt, J.J.E., Bunce, R. G. H., Howard, D. C. & Petit, S. 2002a. General principles of monitoring land cover change based on two case studies in Britain and Denmark. Landscape and Urban Planning 62: 37-51 Brandt, J., De Blust, G., & Wascher, D. 2003. Monitoring multifunctional terrestrial landscapes. In: Brandt, J. & Vejre, H. (eds): Multifunctional Landscapes. Vol. II: Monitoring, Diversity and Management. WITPress, Southhampton, pp. 75-84. Brandt, J., Holmes, E. & Ravn, H. P. 2002b. Biodiversity and trees outside forests: The case of Denmark. 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Springer Verlag, New York, 237pp. Woodward, F.I. & Rochefort, L. 1991 Sensitivity analysis of vegetation diversity to environmental change. Global Ecology and Biogeography Letters 1: 7-23. Table 1. Overview of super categories of Habitat types and the related General Habitats categories (Bunce et al. 2005). Table 2. Examples of species with varying degrees of plasticity. Dwarf Shrubby Low Mid Tall Forest Chamaephytes Chamaephytes Phanerophytes Phanerophytes Phanerophytes Phanerophytes DCH SCH LPH MPH TPH FPH 0.01 – 0.05 0.05 – 0.30 0.30 – 0.60 0.60 – 2.00 2.00 – 5.00 > 5.00 Winter deciduous Salix herbacea X Salix serphyllifolia X Betula nana X X Vaccinium myrtillus X X Myrica gale X X Rosa pimpinellifolia X X Alnus viridis X X X Amelanchier ovalis X X X Salix cinerea X X X X Fragula alnus X X X X Quercus petraea X X X X X Crategus monogyna X X X X X Evergreen Dryas octopetala X Vaccinium oxycoccus X Helianthemum X alpestre Arctostaphylos uva- X X X X ursi Vaccinium vitis-idea Thymus vulgaris X Lavandula stoechas X Siderits syriaca X Helichrsym stoechas X Daphne laureola X Rubus idaeus Vaccinium X X X X X X X X uliginosum Empetrum nigrum X Table 3. Main rules for determining General Habitat Categories and mapping units. GHC’s Mapping Units A GHC has to be determined by one field visit, or from extant data at a scale of at least 1:10,000, which must be made in an appropriate time window for a given region, i.e. either side of the period of maximum biomass. GHC’s must be mutually exclusive and together cover the complete land surface of Europe, including water bodies. GHC’s must be a common denominator for comparison between countries using extant data and classes in current use wherever possible. GHC’s must be distinctive and recognisable. There must be explicit rules to define GHC’s. Differences in management are recorded as qualifiers and are not in the definitions of GHC’s but might influence the delineation of mapping units Habitats are not defined on the basis of biogeographic regions because of difficulties of maintaining consistency due to the lack of adequate definitions of the multiplicity of terms. Any biogeographical term that can be determined consistently can be attached to GHC’s through database management. Individual species are not used to identify GHC’s because of vicarious species and differences in species behaviour in contrasting biogeographical regions. However the use of indicator species to identify environmental qualifiers is useful. The recommended basic survey area is 1 km square within which areal, linear and point elements are recorded. In complex landscapes 0.25 km squares may be appropriate. The key to the General Habitat Categories can however be applied to any extant data or for general recording in the field. The Mimimum Mappable Element (MME) for an areal element is 400 m square with minimum dimensions of 5 x 80 m; if it is smaller than 5 m ( measured as seen in a vertical perspective) the element is recorded as a linear element with a Minimum Mappable Length (MML) of 30 m. Elements that do not pass the minimum size criteria for either areal or linear elements can be mapped and recorded as point elements or as proportions of a larger element. Areal elements with a total extent that passes the MME criteria and lie across the edge of the survey square should be recorded as areal elements even if the part of the element that is within the survey square is below 400 m square. Linear elements of more than 30 m crossing the edge should be recorded if more than 20 m are situated within the area. Roads canals, and broad rivers may be linear elements, but if they are over 400 m square within the survey area and at leeat 5 m wide,they are mapped as aerial elements. (Subsequent database analysis can analyse these as linear elements, if required). Table 4. Procedures and rules for field recording as developed in the BioHab project (Bunce et al. 2005). 1 Surveyors are provided with lists of GHC’s and qualifiers to be used to describe each mapped element (area, line or point) in the survey area. 2 Non-standard secondary codes can be used for site and management qualifiers if the observed site or qualification is not covered by the standard site and management qualifier code listed. 3 The surveyor should record data of areal elements on one recording sheet and data of linear and point elements together on another recording sheet. A third sheet is provided for background information on the survey square. 4 Elements are assigned alpha codes that are the same on the map and on the corresponding recording sheet. Elements with an identical combination of sheet codes can be assigned the same alpha code. 5 The total cover is estimated as from a vertical perspective and the mapping of areal elements adds to 100% of the land surface. The entire survey area must be mapped, even the small corners of the square. 6 Multiple vegetation layers e.g. within forests are not recorded, but could be subject of an additional module within regional surveying activities. 7 Point elements are recorded if they are considered significant in the landscape context. It must be made explicit how these have been recorded, so that they can be monitored effectively. Table 5. Field recording format for European wide recording including qualifiers. Code Field 1 Field 2 Field 3 Field 4 Field 5 Field 6 Field 7 Field 8 α General Habitat Global/ Site Man. Life Form/Species Pan Region Phyto- Category Env. Qualifier Qualifier Europ. al sociolo Class Class gy -1 -1 -1 Qualifier A TPH/DEC/CON NEW 5.3 0 Life Form % Species % 421 TPH/DEC 20 Sor auc 80 429 TPH/CON 10 Pica bi 100 MPH/EVR 60 Rub fru 100 FPH/CON 10 Pica bi 100 Table 6. Definitions of super categories of habitat URBAN/CONSTRUCTED The definition of urban and constructed land codes covers “elements associated with built structure and routes of communication. Linear elements which are immediately adjacent to an urban element are not be recorded, except for roads”. Land is defined as urban, when it “is an area of ground that is associated with a building and which has a use linked to that building e.g. garden”. In most European countries there are clearly marked boundaries around urban land and creation areas e.g. The Netherlands, Spain and Belgium, whereas in other countries e.g. Austria, Estonia and Norway there may not be actual physical boundaries around the houses. Then the urban boundary should be drawn around the grounds of a building where the management intensity changes from that of a gardening character to more extensive management types. CULTIVATED Crops are mainly the product of plant breeding, but also of native specie such as walnut. Wild species collected from semi-natural vegetation are excluded. SPARSELY Elements which have less than 30% cover of vegetation, excluding VEGETATED saxicolous, lichens and bryophytes. HERBACEOUS Herb vegetation if the cover of shrubs and trees is below 30%. They can cover all kinds of vegetation from water plants (helophytes) to bogs (Cryptogams) and grasslands (leafy hemicryptophytes and caespitose hemicryptophytes). SHRUBS AND TREES Most of these habitat categories are woody – the term usually used in habitat classifications – but some chamaeophytes e.g. Phagnalon spp., Artemisia spp., Asparagus spp. Do not have secondary ligneous woody thickening in strict botanical terminology. However, these genera have a shrubby form and have penennating buds above ground level. The woody trees and shrubs refer to individual plants and Life Forms. In the landscape groups of trees and shrubs combine to form forest and shrub habitats. Table 7. Definitions of moisture regimes. Waterlogged/water- Water table at the surface with standing water from between 50 and saturated 70% of the year or with the soil completely saturated. Only small patches may become wet in mid summer. Wet Water table < 40 cm under the surface and soil containing free water for most of the year. Seasonally wet Water table variable at the surface and waterlogged for the winter months or spring flooding season, becoming wet or mesic during the summer period. Mesic Water table 40-100 cm of the surface, available water during most of the non summer period, may dry out during the mid summer period. Dry Water table > 100 cm of the surface, water available only during some periods. Very Dry Water table > 100 cm of the surface, dry throughout most of the year with only short mesic periods. Xeric Water table > 100 cm of the surface, dry throughout the year except in isolated rain events. Table 8. Matrix of nutriant levels (Ellenberg values). Aquatic Water- Seasonally logged wet Wet Mesic Dry Very Xeric Dry Eutrophic 1.1 2.1 3.1 4.1 5.1 6.1 7.1 8.1 Acid 1.2 2.2 3.2 4.2 5.2 6.2 7.2 8.2 Neutral 1.3 2.3 3.3 4.3 5.3 6.3 7.3 8.3 Basic 1.4 2.4 3.4 4.4 5.4 6.4 7.4 8.4 Saline 1.5 2.5 3.5 4.5 5.5 6.5 7.5 8.5 Figure 1. Distribution of the main visits and workshops in the field validation. Figure 2. Biplot of General Habitat Categories (GHC’s) coded as in Section 11 and Environmental Zones (EnZ's) resulting from Canoncial Correspondence Analysis (DCA). The first two axes are shown. Eigenvalue of Axis 1 is 0.42; eigenvalue of Axis 2 is 0.35. The Zones are Alpine North; ALN, Alpine South: ALS, Atlantic North: ATN, Altantic Central: ATC, Lusitanian: LUS, Boreal: BOR, Nemoral, NEM, Continental: CON, Pannonian: PAN, Mediterranean North: MDN, Mediterranean Mountains: MDM, Mediterreanean South: MDS. Figure 3. Diagram of principal potential flows between Life Form categories.